Elisa Hahn on Muck Rack

Elisa Hahn

Seattle
As seen in: Nature, USA Today, KING-TV (Seattle, WA), KHOU-TV (Houston, TX), WKYC-TV (Cleveland, OH), WXIA-TV (Atlanta, GA), WUSA-TV (Washington, DC), KARE-TV (Minneapolis, MN), KGW-TV (Portland, OR), KUSA-TV (Denver, CO) and
Emmy-winning storyteller, former journo, now corporate comms and ⚽️ mom. Retweets are not endorsements. Opinions are my own.
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Articles

Metabolic control of germ layer proportions through regulation of Nodal and Wnt signalling

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By Kristina S. Stapornwongkul, Elisa Hahn, Laura Palau, Krisztina Arato
| biorxiv.org
Abstract During embryonic development, cells exit pluripotency to give rise to the three germ layers. Metabolic pathways influence cell fate decisions by modulating the epigenetic, transcriptional, and signalling states of cells. However, the interplay between metabolism and the major signalling pathways that drive the emergence of ectoderm, mesoderm, and endoderm remains poorly understood.
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Metabolic control of germ layer proportions through regulation of Nodal and Wnt signalling

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By Kristina S. Stapornwongkul, Elisa Hahn, Laura Palau, Krisztina Arato
| tu-dresden.de
Abstract During embryonic development, cells exit pluripotency to give rise to the three germ layers. Metabolic pathways influence cell fate decisions by modulating the epigenetic, transcriptional, and signalling states of cells. However, the interplay between metabolism and the major signalling pathways that drive the emergence of ectoderm, mesoderm, and endoderm remains poorly understood.
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Pharmacological perturbation of the phase-separating protein SMNDC1 - Nature Communications

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By Stefan Gaussmann, Elisa Hahn, Christoph Bock, Georg E. Winter, Michael Sattler, Lennart Enders
| Nature Verified
Abstract SMNDC1 is a Tudor domain protein that recognizes di-methylated arginines and controls gene expression as an essential splicing factor. Here, we study the specific contributions of the SMNDC1 Tudor domain to protein-protein interactions, subcellular localization, and molecular function. To perturb the protein function in cells, we develop small molecule inhibitors targeting the dimethylarginine binding pocket of the SMNDC1 Tudor domain.
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